hereditary spastic paraplegia 64

Summary
Synonym
  • SPG64
  • autosomal recessive spastic paraplegia 64
  • autosomal recessive spastic paraplegia type 64
Definition
A hereditary spastic paraplegia that has_material_basis_in mutation in the ENTPD1 gene on chromosome 10q24.
Super Class
autosomal recessive disease hereditary spastic paraplegia
Related Genes
Displaying 1 entry
Gene ID Gene Symbol Description Source
953 ENTPD1 ectonucleoside triphosphate diphosphohydrolase 1
Displaying 1 entry
Gene ID Gene Symbol Description Source
12495 Entpd1 ectonucleoside triphosphate diphosphohydrolase 1
The Human Phenotype Ontology
Displaying entries 11 - 16 of 16 in total
HPO ID HPO Term
HP:0002342 Intellectual disability, moderate
HP:0003202 Skeletal muscle atrophy
HP:0001249 Intellectual disability
HP:0000007 Autosomal recessive inheritance
HP:0001762 Talipes equinovarus
HP:0000519 Developmental cataract
Displaying 1 entry
Gene ID Gene Symbol Description
953 ENTPD1 ectonucleoside triphosphate diphosphohydrolase 1

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Acknowledgements

Supported by JST NBDC Grant Number JPMJND2204

Partly supported by NIH Common Fund Grant #1U01GM125267-01


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Last updated: December 9, 2024